- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
8 result(s) found for: Cellulose.
Displaying page 1 of 1.
EudraCT Number: 2004-001054-84 | Sponsor Protocol Number: 2004/W/GI/02 | Start Date*: 2005-02-16 |
Sponsor Name:NHS Lothian- University Hospitals Division | ||
Full Title: A comparison of the efficacy of dietary hydroxypropylcellulose and questran as therapeutic agents in bile acid induced diarrhoea | ||
Medical condition: these patients will have bile acid induced diarrhoea identified by an increased serum 7a-OH-cholestenone. and will have a history of one of 1. ileal resection 2. idiopathic bile acid diarrhoea.3. ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002507-28 | Sponsor Protocol Number: OPHT-280515 | Start Date*: 2015-07-20 | |||||||||||
Sponsor Name:Medical University of Vienna | |||||||||||||
Full Title: Effect of benzalkonium chloride containing eye drops on the conjunctival bacterial flora of dry eye patients. | |||||||||||||
Medical condition: conjunctival bacterial flora in patients with dry eye syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006846-24 | Sponsor Protocol Number: HTA074801 | Start Date*: 2009-02-27 |
Sponsor Name:North West London Hospitals NHS Trust | ||
Full Title: An Evaluation of the Effectiveness of Ibuprofen and Morphine for Acute Pain in Sickle Cell Disease | ||
Medical condition: Sickle Cell Disease | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001725-75 | Sponsor Protocol Number: 2015-DFU-301 | Start Date*: 2018-12-12 |
Sponsor Name:FirstString Research, Inc. | ||
Full Title: A Phase 3, Randomized, Double-blind, Parallel-group, Vehicle controlled, Multicenter Study of the Efficacy and Safety of Granexin Gel in the Treatment of Diabetic Foot Ulcer (GAIT 1) | ||
Medical condition: Diabetic Foot Ulcer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000328-42 | Sponsor Protocol Number: CP-104 | Start Date*: 2007-08-03 | |||||||||||
Sponsor Name:Arrow Therapeutics Ltd | |||||||||||||
Full Title: A clinical pharmacology study to determine the pharmacokinetic , safety and tolerability profile and antiviral activity of multiple oral doses of A-831 in otherwise healthy male Hepatitis C carrie... | |||||||||||||
Medical condition: Male Hepatitis C carriers with compensated liver disease | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017481-23 | Sponsor Protocol Number: SPD09P1401 | Start Date*: 2010-10-15 | |||||||||||
Sponsor Name:SmartPractice | |||||||||||||
Full Title: Clinical Evaluation of T.R.U.E. TEST® Neomycin Sulfate and Potassium Dichromate Allergens: Bioequivalence of Vehicle Formulations | |||||||||||||
Medical condition: Diagnosis of Allergic Contact Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001878-29 | Sponsor Protocol Number: 35RC18_8852_PROPRADO | Start Date*: 2021-05-21 | |||||||||||
Sponsor Name:Rennes University Hospital | |||||||||||||
Full Title: The efficacy of traumatic memory modification using a memory reconsolidation procedure under propranolol among adolescents with post-traumatic stress disorder (PROPRADO) | |||||||||||||
Medical condition: post-traumatic stress disorder | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000937-54 | Sponsor Protocol Number: MC2-03-C1 | Start Date*: 2015-08-03 | ||||||||||||||||
Sponsor Name:DRUG DELIVERY SOLUTIONS ApS (PART OF MC2 BIOTEK GROUP) | ||||||||||||||||||
Full Title: A phase II, multicenter, randomized, double-masked, 4 parallel arms, controlled 6-month trial designed to evaluate the safety and efficacy of PAD ciclosporin (CsA 0.06% and 0.03%) ophthalmic disper... | ||||||||||||||||||
Medical condition: ocular dryness (Dry Eye Disease - DED) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) DK (Completed) NO (Completed) AT (Completed) ES (Completed) PT (Completed) FR (Completed) SK (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
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